A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17153835



Internal ID21482381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101804362..101804362hg38UCSC Ensembl
chr8:102816590..102816590hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5634142
Supporting Variants
SamplesHG03732
Known GenesNCALD
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17153835
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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